nsv959315
- Organism: Homo sapiens
- Study:nstd86 (Poultney et al. 2013)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: No
- Region Size:68,726
- Publication(s):Poultney et al. 2013
Source: NCBI
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 324 SVs from 54 studies. See in: genome view
Overlapping variant regions from other studies: 324 SVs from 54 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Inner Start | Inner Stop |
|---|---|---|---|---|---|---|---|---|---|
| nsv959315 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000004.12 | Chr4 | 103,589,680 | 103,658,405 |
| nsv959315 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000004.11 | Chr4 | 104,510,837 | 104,579,562 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis |
|---|---|---|---|
| nssv3021256 | duplication | Sequencing | Read depth |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Inner Start | Inner Stop | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|---|---|
| nssv3021256 | Remapped | Perfect | NC_000004.12:g.(10 3196852_103589680) _(103658405_103719 126)dup | GRCh38.p12 | First Pass | NC_000004.12 | Chr4 | 103,196,852 | 103,589,680 | 103,658,405 | 103,719,126 |
| nssv3021256 | Submitted genomic | NC_000004.11:g.(10 4118009_104510837) _(104579562_104640 283)dup | GRCh37 (hg19) | NC_000004.11 | Chr4 | 104,118,009 | 104,510,837 | 104,579,562 | 104,640,283 |